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N-杂环卡宾催化的通过α,β-不饱和酰基唑鎓的对映选择性合成螺戊二酰亚胺。

N-Heterocyclic Carbene-Catalyzed Enantioselective Synthesis of Spiro-glutarimides via α,β-Unsaturated Acylazoliums.

机构信息

Organic Chemistry Division , CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road , Pune 411008 , India.

Academy of Scientific and Innovative Research (AcSIR) , New Delhi 110020 , India.

出版信息

Org Lett. 2018 Aug 3;20(15):4499-4503. doi: 10.1021/acs.orglett.8b01799. Epub 2018 Jul 26.

Abstract

NHC-catalyzed enantioselective [3 + 3] spiro-annulation of α,β-unsaturated aldehydes with cyclic β-ketoamides allowing the preparation of synthetically and biologically important spiro-glutarimide derivatives has been reported. The interception of the ketoamides with catalytically generated chiral α,β-unsaturated acylazoliums proceeds in a Michael addition-intramolecular amidation pathway to deliver the spirocyclic products with good yield, diastereoselectivity, and enantioselectivity.

摘要

NHC 催化的 α,β-不饱和醛与环状 β-酮酰胺的对映选择性[3+3]螺环化反应,可制备具有重要合成和生物意义的螺环戊二酰亚胺衍生物。催化生成的手性 α,β-不饱和酰基氮鎓中间体与酮酰胺的加成-分子内酰胺化反应,以良好的收率、非对映选择性和对映选择性得到螺环产物。

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